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FDA Compliant HPLC Qualification and Performance Testing

 
  February 25, 2010  
     
 


GlobalCompliancePanel, Online
March 4, 2010


Learn how to select, conduct and document the right tests in the right sequence. High Performance Liquid Chromatography is the most frequently used analytical tool for pharmaceutical and API testing laboratories. FDA and international agencies require HPLC equipment to be calibrated, qualified and tested to ensure accurate and reliable analytical results. Even though this is well known since long time, laboratories are unsure on what exactly should be tested initially and on an on-going basis. The main challenge is to do the right testing in the right sequence.
 
 
Organized by: GlobalCompliancePanel
Invited Speakers: Dr. Ludwig Huber
Chief Advisor - Global FDA compliance, Agilent Technologies

Ludwig Huber, Ph.D., is Director of Labcompliance and Chief Advisor for global FDA compliance at Agilent Technologies. He is the editor of Labcompliance, the global on-line resource for validation and compliance issues for laboratories. He is the author of the books "Validation and Qualification in Analytical Laboratories, and "Validation of Computerized Analytical and Networked Systems", Informa Healthcare.
 
Deadline for Abstracts: March 2, 2010
 
Registration:
Thursday, March 4, 2010  
10:00 AM PST | 01:00 PM EST
Live live online training only for one participant
Price: $245.00
 
 

Corporate Live 4 to 10 participants from a single location (For multiple locations contact Customer Care)
Price: $995.00
E-mail: webinars@GlobalCompliancePanel.com
 
   
 
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